Author: BIOS Consortium

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Preprints

Unraveling the polygenic architecture of complex traits using blood eQTL meta-analysis

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A linear mixed model approach to study multivariate gene-environment interactions

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  • In genetics: 267
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Deconvolution of bulk blood eQTL effects into immune cell subpopulations

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Genetic predisposition to mosaic Y chromosome loss in blood is associated with genomic instability in other tissues and susceptibility to non-haematological cancers

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  • In genetics: 651
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Identification of 370 loci for age at onset of sexual and reproductive behaviour, highlighting common aetiology with reproductive biology, externalizing behaviour and longevity

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  • Site-wide: 18,443
  • In genetics: 904
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RNA-Seq in 296 phased trios provides a high resolution map of genomic imprinting

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An epigenome-wide association study of educational attainment (n = 10,767)

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Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus.

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Novel blood pressure locus and gene discovery using GWAS and expression datasets from blood and the kidney

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  • In genomics: 2,811
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Genome-wide identification of directed gene networks using large-scale population genomics data

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Genomic and phenomic insights from an atlas of genetic effects on DNA methylation

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  • Site-wide: 35,407
  • In genetic and genomic medicine: 109
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Genome-wide identification of genes regulating DNA methylation using genetic anchors for causal inference

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  • Site-wide: 49,370
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The role of gene expression on human sexual dimorphism: too early to call

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Correction for both common and rare cell types in blood is important to identify genes that correlate with age

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  • In bioinformatics: 7,832
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DNA methylation signatures of aggression and closely related constructs: A meta-analysis of epigenome-wide studies across the lifespan

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  • Site-wide: 95,754
  • In genetics: 4,291
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Triangulating molecular evidence to prioritise candidate causal genes at established atopic dermatitis loci

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Imbalanced expression for predicted high-impact, autosomal-dominant variants in a cohort of 3,818 healthy samples

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  • Site-wide: 120,151
  • In genomics: 6,577
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Genome-wide study of DNA methylation in Amyotrophic Lateral Sclerosis identifies differentially methylated loci and implicates metabolic, inflammatory and cholesterol pathways

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  • In neurology: 533
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